Technical review on the issuance of cosmetics and cosmetic points of the technical review of guidelines to inform

State Food and Drug Administration Xu [2010] 393
September 28, 2010 release

Review of the State Food and Drug Administration Center:

To further standardize the technical review of administrative licensing cosmetics, ensure that the administrative permit open, fair, impartial, National Bureau of organizations to develop a "technical review of cosmetic points" and "cosmetic technology review guidelines", are hereby issued, please comply.

Attachment:

1. Elements of the technical review of cosmetics
2. Cosmetics technical review guidelines

State Food and Drug Administration
二○一 ○ 年 九月 二十 八日

Annex 1:
Elements of the technical review of cosmetics

Chapter I General Provisions

The first technical review to regulate cosmetics, cosmetics administrative licensing to ensure open, fair, just, to develop the technical review points.

The second point of this technical review report for the first time, the administrative licensing work of the technical review of special use cosmetics.

Article cosmetics shall comply with the technical review, "Cosmetics Health Supervision" and the relevant laws and regulations, standard specifications, in accordance with relevant regulations, in accordance with the principles of risk assessment, based on science.

Article IV of the technical review shall be in accordance with legal procedures, to follow the statutory time limit and improve efficiency.

Article cosmetics technical review of the findings or results, shall open.

Technical requirements of Chapter

Article VI declarations should be real, legitimate, its content and form of administrative license shall meet the cosmetic requirements declaration accepted.

Article shall meet to declare the product category "Cosmetics Health Supervision" and its Implementing Rules and other relevant provisions of the definition and scope of requirements.

Article application form should be complete and its contents should include basic product information and production companies, special circumstances should be explained in another column to explain the problem.

Article IX product formulation should contain material number, the name of the international cosmetics ingredients (INCI name) (domestic products), the standard Chinese name, percentage content, the intended use and so on. Compound compound in the form of raw materials should be declared (except fragrance). Meanwhile, the product formulation should also provide the Chinese name of the product, imported products should also provide foreign language name.

Article product quality and safety control requirements should include the declaration of the actual control of the product indicators and their specific control requirements, and commitment to the product specifications in line with our cosmetic health.
If the implementation of the national domestic product standards or industry standards, should also explicitly declare the control related to product quality and safety indicators specific requirements.

Article XI of foreign imported products should provide the original packaging commercial products (including product labels, product instructions), and faithfully translated into standard Chinese. Intended for the Chinese market, packaging design, product design, packaging must also be submitted (including product labels, product instructions). Imported products and foreign language content should be declared labels, instructions on use, the use of population and consistent with other parts.
Declaration should be made to provide product design, packaging products (including product labels, product instructions).

Article XII of the Chinese product label instructions should be consistent with label instructions on the management of cosmetic regulations. Chinese name of the product shall meet the requirements of cosmetics named.

Article XIII of the administrative claims data in the cosmetics licensing inspection reports shall meet the Hygienic Standard for Cosmetics and cosmetic inspection standard and other relevant administrative licensing requirements.

Article XIV declared the product may be a security risk assessment of material safety data should be consistent with cosmetics possible security risk substances risk assessment guidelines and requirements.

Article XV for the efficacy of ingredients used should be based on relevant experimental reports or published scientific literature, test reports or the relevant scientific literature should clearly support the efficacy claims.

Article XVI claims data in the production and sale documents, materials and other specifications that documents issued by third parties should be real, legitimate, and meet the relevant requirements.

Chapter III to determine the principles of

Article XVII of cosmetics products comply with relevant laws and reporting regulations, standards requirements, and meet the requirements of the technical review, judged to be "recommended for approval."

Article 18 to declare the product one of the following conditions, determine the "additional information, delayed retrial":
(A) the need to add test;
(Ii) the need to provide explanation of the reporting unit;
(C) to be issued by a third-party documents;
(D) other changes, additional information of the situation.

Article 19 declaration of products meet the following circumstances, judged to be "does not recommend approval":
(A) reporting false information or samples.
1. Product formula information other than to declare types of raw materials used in production or formulation is inconsistent with the declared content;
2. Components declared in the product formulation or content type does not match with the actual test results;
3. Third parties to provide false documents;
4. Provide samples or false submission of samples to trial;
5. Truthful disclosure of information in foreign languages ​​are not translated into Chinese, affect the conclusions of the review;
6. Inconsistent with the original copy of the content;
7. Reporting false information or samples of other situations.
(B) the cosmetic product formulations do not meet hygiene standards required.
1. Cosmetics, health products formulated with the specification of the prohibited substances;
2. Product formulations restricted substances, sunscreen agents, coloring agents, preservatives, dyes and other cosmetics, hygiene does not meet regulatory requirements.
(C) the test results do not meet hygiene standards of cosmetics and related provisions; toxicology test results showed that the product has potential safety issues; test results do not meet the reporting requirements of product quality and safety control.
(D) based on claims data can not determine the safety of products, and can not continue within the time limit to complete safety evaluation.
(E) the production health conditions do not meet audit requirements, or other on-site audit results do not meet the requirements.
(F) product category with the relevant provisions of the declaration is inconsistent.
(Vii) additional information from reporting units to change their own product formulations, production processes, product quality and safety control requirements, etc., affect the conclusions of the review.
(H) has made recommendations not to approve the findings from the review of the product, review units of their own when to change the product's original reporting claims data.
(I) the product type and content of raw materials, formulations and product range of quality and safety control requirements in the corresponding content is not consistent.
(X) production process of raw materials and product formulations in the corresponding content inconsistent.
(K) to declare health conditions, product formulation and production audit of the formula or formula recognized testing agencies licensed in the types of raw materials, content and purpose of use is not consistent.
(12) other non-compliance with the relevant regulations.

Chapter IV Supplementary Provisions

Diershitiao this point the technical review by the State Food and Drug Administration responsible for the interpretation.

Article cosmetics procedures to declare a failure of the product, not the technical review, in accordance with relevant regulations.

Article 22 of the technical review of new cosmetic raw material requirements separately.

Article 23 of the main points of the technical review of health supervision and law enforcement not as the basis for cosmetics.

Article 24 The technical review of key points from the release date of implementation.

Annex 2:
Cosmetics technical review guidelines

In order to regulate cosmetics technical review, according to the Hygienic Standard for Cosmetics, cosmetics declaration accepting the administrative licensing requirements and other cosmetic elements of the technical review of the technical review of the development of this guide.

First, the Chinese name of the product
Product name Chinese name should be consistent with the provisions of cosmetics, cosmetics naming guidelines.
(A) the name should be provided in the report based on the product's brand name, common name (including the intended use or use parts), interpretation of the meaning of specific attribute name. Convention, the name can be used to omit the use of cosmetics, common name, property name.

(B) the product if that product in the Chinese name or the appearance of morphological and physical properties including color, color, SPF, odor, for hair, skin or other content of specific populations, should be explained.

(C) the product name in the Chinese name if the use of specific raw materials or that category of words, should be explained.

(D) the modification of the product in the Chinese name, adjective, or to use foreign letters, symbols, etc., should be explained.

Second, the sample sent for screening
(A) the product packaging should be complete, imported products should be commercially available for the unopened package. Package should include product specifications, because of their size too small (such as lipstick, lip balm, etc.) without the contents of the product manual or instructions printed on the product container should be part of the claims data are described in the product packaging.
Imported samples should be affixed on the packaging marked with the Chinese name of the product label, must not cover all the foreign labels.
Domestic product sampling and sample letters, sample letters should be imported cosmetic products on the administrative licensing requirements of implementation.

(B) submitted for review samples of the product packaging (including product labels, product instructions) for disclosure of information content should be consistent with the relevant information, such as the inspection sample batch, use the deadline date or production date and shelf life.

Third, the product formula
(A) general requirements of the product formula
1. Product formulations should be the product name, imported products should be Chinese (translated) name. Product formulations should be in tabular form in the same table contains the raw numbers provided, the name of the international cosmetics ingredients (INCI name) (domestic products), raw material standard Chinese name, percentage content, purpose of use, etc., size is not smaller than Times New Roman五号.
Domestic product formula to produce sanitation review subject to product formulations available; imported products formulated to permit inspection agency to confirm the product formulas prevail.
2. Product formulation should provide the name of all raw materials, the actual content of the percentage, and indicate the effective matter content (not caught in an effective matter content indicated 100%); compound materials (except fragrance) should be the form of compound returns, and should indicate which of the components in the content (in%); special circumstances, such as those containing crystal water, raw materials, there are different formula or structure type, and so should be described, all materials in descending order according to content.
3. Product formulation of raw materials used in flavor, you can declare the amount of flavor in the recipe, not required to report the specific spice flavor components of the type and content, material name to "flavor" name. Such as fragrance and flavor while reporting component type and content of spices, the fragrance raw materials should be submitted on company issued all of the flavors and fragrance components contained in the type and content of documents. Documents are in foreign languages ​​should be translated into Chinese, and Chinese translations notarized.
The use of raw materials to declare the purpose of the product should be based on raw materials in their products, the actual role of the mark, for example: emollients, emulsifiers, solvents, preservatives, etc., but may not use medical terminology.
4. Formula components (including compound ingredients in each component) of the Chinese name should be the international standard cosmetic ingredients using a standard Chinese name Chinese name directory. No INCI name included in the international cosmetics raw materials or standard Chinese name directory, you should use the name in the Chinese Pharmacopoeia or plants or chemical name Latin name, common name or trade name not be used, but except for compound materials.
5. Cosmetic colorant hygiene practices should be provided on the coloring agent contained in the index number (referred to as CI No.), except no CI number.
6. After review of the production health conditions or license the product formula recognized inspection agency can not modify product formulations.
7. Multicolor number series sunscreen cosmetics, when the same basic formula, and apply the sunscreen (SPF, PFA or PA) test, it can also make a declaration as a product.
Each product dossier should be accompanied by the list of products, basic recipes and a list of coloring agents and the list of sample products; not detect the product dossier should indicate where the sample product test reports the name of Chinese products and to provide a sample product test copies of the report.
8. Two or two or more must be used in conjunction with the product, a product should be declared. Are mixed according to multi-dose use of the actual situation, or to submit inspection reports were submitted to mixed formulations of the respective inspection reports.
9. Purporting to pregnant women, lactating women, children or infants products, security considerations should be based design principles of product formulations (including formulations overall analysis), the choice of the principles and requirements of raw materials, production processes, quality and safety control content information.

(B) the product formulation raw material requirements
1. Cosmetic product formulation should not be used to disable health component specification.
2. Product formulations are cosmetic raw materials, such as health specification restricted substance, shall not exceed the requirements of the appropriate (to) with the scope, restrictions, requirements and limits.
3. Product formulations labeled as preservatives, cosmetics, hygiene practices should be in line with the relevant requirements.
4. Sunscreen formulations labeled sunscreens, cosmetics, hygiene practices should be in line with the relevant requirements.
Non-UV absorbers in sunscreen products used to protect the product, the type of UV absorber can be restricted from use in cosmetics, hygiene practices sunscreen limit, but its use should be assessed by security, and prove its security.
5. Product formulations should be used in coloring cosmetics hygiene practices require the use of coloring agents, and shall comply with its provisions.
6. Where the Hygienic Standard for Cosmetics in the quality of materials used for the required specifications, raw materials should be provided by the manufacturer that the specifications issued by (foreign raw materials to produce the legal representative or legal representative of the manufacturer's authorized signatory of the signature or official seal cap manufacturer ). Cosmetic quality specifications generally include the contents of health regulatory requirements. Reporting the use of petroleum products lysate formula based raw materials, should provide the Chemical Abstracts index of raw materials (referred to as CAS number).
7. Denatured alcohol used in product formulation, it shall indicate the name and adding the amount of denaturant.
8. Permanent and semi-permanent hair color products used in dyes, coupling agents and dyes intermediates, cosmetics, hygiene practices should be in the temporary use of hair dyes (except those already approved for use in another), and shall comply with its provisions.
9. Product formulations and the use of animal organs and tissues extracts of blood products as raw materials, should declare their source, quality specifications and allows the use of raw materials to produce proof of the country.

(C) the effectiveness of the composition requirements
1. Apply for Hair, body, breast products, and should indicate the effectiveness of the composition and use basis. Effectiveness of the composition should be based on experiments using reports or published scientific literature, test reports or the relevant scientific literature should be clearly supported the efficacy of reporting claims.
2. Effectiveness of the composition of plant extracts, the extraction process should be provided or quality specifications, including their considerable amount of the original plant or solids content, solvent extraction and variety of content and other indicators.

Fourth, the production process requirements
(A) to provide the production process should include the process description and process diagram, process description should be concise and reflect the product's actual production process, including steps, the steps involved in raw materials. All material product formulations should be listed in the production process, raw materials and product formulations should be the same name.

(B) the process description and process diagram should be consistent.
Fifth, the product quality and safety control requirements
(A) Product quality and safety control requirements should be color, character, smell and other sensory indicators.

(B) the quality and safety indicators should include microbiological indicators (except without detection) and chemical indicators of health.

(C) the unit of measurement of indicators should be consistent with the relevant requirements of Hygienic Standard for Cosmetics.

(D) Product quality and safety control requirements in the type and content of the raw materials involved in the scope should be consistent with the product formula, cosmetics, hygiene practices also meet the relevant requirements.

(E) class perm, hair type, freckle-containing products and the claims, though not of α-hydroxy acid or α-hydroxy acid containing claims, but the total amount of ≥ 3% (w / w), the product should be pH value indicator [water in oil (oil-like product), powder, powder type, except wax-based class], and also indicate the test method.

(F) product quality and safety control requirements should include the declaration of the actual control of the product indicators and their specific control requirements. Imported products and foreign-language versions should be submitted to the Chinese translation. Implementation of country of origin product quality and safety control requirements in the non-paragraphs (a), (b), (e) the content, should be submitted simultaneously with the corresponding indicator of product quality and safety control requirements information.

(G) The applicant shall submit the product specifications in line with the commitment of cosmetics health.

6, the product packaging (including product labels, product brochures)
(A) product design packaging (including product labels, product brochures)
1. Product labels should be marked the following:
(1) Chinese name of the product.
(2) use of the product lot number and deadline date or production date and shelf life.
(3) Net content.
(4) The name and address of manufacturer:
Domestic product registered according to law should be marked, and assume responsibility for quality and safety of cosmetic hygiene manufacturer name and address;
Country of origin of imported products should be marked or region (referring to China, Hong Kong, Macao and Taiwan) the name and registered according to law in China, the agent, importer or distributor's name and address.
(5) domestic product manufacturer should be marked health license number.
(6) marked by cosmetic regulatory requirements related health conditions of use, cautions or warning language. If necessary, mark the use of cosmetics for people and the use of parts and so on.
2. Product packaging (including product labels, product instructions) marked by the name of raw materials, involving content should be consistent with the product formula.
3. Product packaging (including product labels, product instructions) shall contain the following:
(1) indications, efficacy, medical terminology;
(2) antimicrobial, antibacterial, sterilization, sterilization, disinfection and other content;
(3) the use of the name of others or to suggest ways to ensure its effectiveness misleading;
(4) the effectiveness of claims beyond the scope of its definition;
(5) "approved by the Ministry of Health" or "by the State Food and Drug Administration approval," the name of, or in cosmetics and other inspection bodies and inspection reports the name of publicity;
(6) false hype to mislead and deceive consumers;
(7) Other laws and regulations, standards and norms prohibited content.
4. Mark PFA value (long-wave ultraviolet protection factor) or PA + ~ PA + + + sunscreen products should be detected PFA value; claim UVA protective effect or claim broad-spectrum sun protection products should be tested for anti UVA ability parameters - critical wavelength (Instrumental), or determination PFA value (body method), the critical wavelength test results greater than or equal to 370nm can be marked broad-spectrum, less than 370nm broad-spectrum shall not marked.
5. SPF of sunscreen products should be marked as follows:
(1) Sunscreen products can not label SPF value;
(2) the measured products with SPF values ​​less than 2, no marked effect of sunscreen;
(3) of the measured products with SPF values ​​between 2 to 30 (including 2 and 30), the label shall not exceed the value of the measured value;
(4) of the measured products with SPF values ​​greater than 30, and subtracting the standard deviation is still greater than 30, the maximum can only be marked SPF30 +, may not mark the measured values; the test products with SPF values ​​greater than 30, after subtracting the standard deviation less than or equal to 30, the maximum can only be marked SPF30.
Claimed waterproof sunscreen products should be labeled SPF value after the bath if the bath while before the label SPF value should be specified. If the bath with the SPF value determined after the bath before the determination of the SPF value of 50% reduction compared, then the mark may not waterproof. Chinese name of the product has waterproof and sweat in such terms, shall not be labeled SPF value before the bath.
6. PFA value of sunscreen products should be marked as follows:
(1) the measured value of the product integral part of the PFA is less than 2, no marked effects of UVA sun protection;
(2) product integral part of the PFA in the measured values ​​of between 2 to 3 (including 2 and 3), PA + can be marked or measured values ​​of the integer part of the PFA;
(3) product integral part of the PFA in the measured values ​​of between 4 to 7 (including 4 and 7), PA + + can be marked or measured values ​​of the integer part of the PFA;
(4) product integral part of the PFA is greater than the measured value is equal to 8, can be marked or PFA PA + + + integer part of the measured values.
Product labels, product instructions) have built-in manual display, or disclosure of information in the sample submitted for review should be built-in instructions.
5. Original packaging (including product labels, product instructions) if the product in the Chinese name, Chinese name should return the product to its line. Product disclosure of information in the original Chinese name and the product packaging does not match the Chinese name should be in the Chinese label instructions marked "original packaging Chinese name × × × × × × regional sales for the names."
6. Original packaging (including product labels, product instructions) marked the SPF, PFA or PA SPF values ​​higher than detection, PFA or PA values, norms and cosmetic hygiene should be the requirements of the relevant provisions in the Chinese labels, instructions be marked.
7. In addition to trademarks and the need to use foreign letters, symbols of the information, the import of cosmetics original packaging (including product labels, product instructions) are all translated content should be marked correct, standard Chinese. Audit to Chinese packaging products (including product labels, product brochures) shall prevail. If necessary, refer to the product of the original packaging (including product labels, product instructions) content.
(1) original packaging (including product labels, product instructions) marked "acne, anti acne, prevent, or does not cause acne," and other related content, to declare the project should provide antibiotics and metronidazole test report.
(2) hair products original packaging (including product labels, product instructions) marked "dandruff" purposes, declare the project should be to provide anti-dandruff agent test report.
(3) sunscreen products original packaging (including product labels, product instructions) label SPF value, PFA value, PA value, UVA protection, or declaring that "waterproof", "sweat" or "suitable for swimming and other outdoor activities" and other related content , reporting should provide SPF, PFA, UVA protection, test reports or waterproof sunscreen products test report, and shall regulate cosmetics and health-related provisions in the Chinese label instructions to be on the mark.
Above shall provide the appropriate test or test reports, not by modifying the original packaging (including product labels, product instructions) and marked reduction test pilot project.
(4) original packaging (including product labels, product instructions) if the label "medicinal", "medicine" and Chinese characters (including Traditional Chinese), or labeling of medical terminology, claiming health effects, suggesting the efficacy or false hype, which do not meet the China's relevant regulations and requirements of the content, the Chinese should be in the product label instructions be an explanation.

Seven, chemical and microbiological testing Health
(A) permit inspection application form, notification of acceptance testing, product specifications and inspection reports in the Chinese name of the product and reporting unit name should be the same. If the administrative licensing application form with the product name and Chinese name of inconsistent reporting unit shall be submitted to permit inspection agency issued the additional inspection reports and the reasons.

(B) permit application forms and testing the product inspection reports in color, physical properties and product quality and safety control should be the relevant requirements in line.

(C) permit application forms and inspection reports testing the product lot number should be consistent.

(D) health and chemical test results should be product formulations and product quality and safety control requirements and the requirements of component content in the corresponding line.

(E) cosmetics hygiene standards required in the finite, the corresponding measured values ​​must not exceed specified limits.

(F) test the administrative licensing items shall meet the test specifications of cosmetics, health chemical testing program, microbiological and toxicological testing program pilot project should be in the same health and safety inspection of licensed inspection agency.

(G) multi-color No. products, cosmetics, administrative license shall be tested according to specifications for each product microbiological and chemical testing health.

(H) multi-dose hair type, perm products of chemical indicators of health should be measured separately. Product formulations without inhibition of microbial products (including physical hair removal products, deodorant products, etc.) should be measured microbial indicators.

(I) product formulation products containing talc should be provided with a measurement certification inspection agency issued a qualified report the detection of impurities in the report of asbestos products.

Eight, toxicology safety evaluation
(A) the audit points
1. Licensing test application, test the notification of acceptance, product specifications and inspection reports in the Chinese name of the product and reporting unit name should be the same. If the administrative licensing application form with the product name and Chinese name of inconsistent reporting unit shall be submitted to permit inspection agency issued the additional inspection reports and the reasons.
2. Permit application and inspection test report the product color, physical properties and product quality and safety control should be consistent with requirements.
3. Permit inspection and inspection report, the application form should be the same product lot number.
4. Before testing for human safety should be the first to complete toxicology tests and issued the necessary documentary evidence, toxicology test samples failed safety tests on humans may not.
5. Sunscreen products should meet the following requirements:
(1) packaging (including product labels, product manual), whether labeled SPF value sunscreen products should be required by the Hygienic Standard for Cosmetics test SPF value;
(2) to the function of the foreign laboratory test reports sunscreen cosmetics, cosmetics administrative license shall require the request for declaration of acceptance;
(3) The number of products for multi-color, sample data are sampling problems, then while reporting on the number of multi-color products for the appropriate treatment.

(B) the results to determine the principles of
1 declare animal testing of products may not appear obvious skin irritation, corrosion and eye irritation, corrosive, infants, children should be strict with the product requirements.
2. Declare animal testing of products may not appear obvious skin allergy and skin phototoxicity.
3. Mutagenic product portfolio reporting test should be negative.

Nine, human safety evaluation
Human safety testing of cosmetics administrative licensing items shall meet the test specification requirements.
(A) non-rinse products after use, health and safety test results pH ≤ 3.5 or product quality and safety control requirements set pH ≤ 3.5 in the product should be test for human safety trial. Test substances may have adverse effects on the human body.

(B) human closed patch test
Deodorant category, freckle, sunscreen products, the body should be closed patch test.
30 cases of subjects appear in a number of skin reactions and not more than 5 cases (excluding 5 cases, the same below), or 2 skin reactions of a number not more than 2 cases (patch test a deodorant product The number of skin reactions grade not more than 10 cases, two skin reactions of a number not more than 5 cases), or not 1 case of grade 3 or grade 3 skin reactions.

(C) open skin patch test
Powder (such as powder, foundation, etc.) special cosmetics for skin patch test, the results appear irritating or difficult to judge the results, it should increase the open patch test.
30 cases of subjects in a skin reactions and not more than 5 cases (including 5 cases, the same below), 2 skin reactions and not more than 2 cases, or may not occur more than 3 or 3 1 cases of skin reactions above.

(D) safety evaluation of human pilot trial
Hair type, body type, breast and hair removal products like human trial test should be carried out safety assessment.
1. Hair class, fitness classes and Breasts class products 30 subjects appear in a number of skin reactions and not more than 2 cases (excluding two cases, the same below), or 2 skin reactions of a number not more than 1 case, or not 1 case of grade 3 or grade 3 skin reactions.
2. Hair removal products in 30 cases the subjects may not appear for more than three cases (excluding 3 cases, the same below) a skin reactions, skin reactions or two the number of not more than 2 cases, 1 case or not three and three or more skin reactions.

(E) human safety inspection program should be licensed with a human safety inspection agency inspection.

Ten, cosmetics possible security risk substances risk assessment information
(A) there may be cosmetic safety risk assessment information to review the material shall conform to the safety of cosmetics that may exist in material risk assessment guidelines.

(B) the audit points
1 cosmetics under a security risk may exist in material risk assessment guidelines, hazard identification through the analysis of the undertaking to be recognized; without undertaking the analysis of hazard identification, not recognition.
2 Risk Assessment Report by the hazard identification analysis, the product may contain a security risk materials, should provide security risks in the product material content of the inspection report, or raw material content in the test reports or quality of raw material specifications ( including the substance of the content requirements). Quality of raw material specifications provided by manufacturers of raw materials and official seal (the legal representative of the foreign producers of raw materials or the legal representative of the manufacturer's signature or signature cap seal manufacturer). If the information provided foreign language, to be translated into standard Chinese. Involving dioxane, dioxane to provide risk assessment information only dioxane content of test reports or quality of raw material specifications.
3 relevant foreign authority has established limit values ​​or have been related to evaluation findings, can provide the latest version of the safety evaluation report and other relevant parts of the original copy of the data and translated into standard Chinese.
Foreign official or regulations have been issued a security risk for some substances have limited requirements, the need to provide appropriate information and translated into standard Chinese copy.
4. A raw material manufacturer of the product of all materials issued by the formula does not contain any substances of general security risk guarantee, does not endorse. Should be based on material properties, respectively for instructions.

XI Other
(A) This technical review guidelines for health supervision and law enforcement not as the basis for cosmetics.
(B) does not meet the administrative licensing inspection reports and the relevant provisions of the Hygienic Standard for Cosmetics, the cosmetics according to the technical review by the views of the applicant, to the appropriate inspection agencies, inspection agencies should be the administrative licensing regulations.
(C) the technical review is not limited to the technical requirements of the contents of the review guidelines, guidelines for the review of this technology outside the scope of other relevant content, should state the relevant provisions of cosmetics.
(D) of the State Food and Drug Administration according to the administrative licensing work of cosmetic need, otherwise the development of relevant regulations.

  

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